Allele Registry

Canonical Allele Identifier: PA317627

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189008

RCV001067049

ClinVar Variation:

206870

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Met1845Thr	CA317625 NM_006920.6:c.5534T>C